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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494629Generated: October 30, 2026

Triethylamine → 1-[5,5-Bis(4-fluorophenyl)-4-pentenyl]-4-(phenylmethyl)-2-piperazinecarboxamide

https://huagongshe.com/reaction/1494629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Benzylpiperazine-2-carboxamideHCID 14230266—
Reactant5-Bromo-1,1-bis-(4-fluorophenyl)pent-1-eneHCID 14722550—
SolventDimethylformamideHCID 6228—
Product1-[5,5-Bis(4-fluorophenyl)-4-pentenyl]-4-(phenylmethyl)-2-piperazinecarboxamideHCID 1982844561.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 74.2 parts of 1,1'-(5-bromo-1-penten-1-ylidene)bis[4-fluorobenzene], 43.8 parts of 4-(phenylmethyl)-2-piperazinecarboxamide, 38.9 parts of N,N-diethylethanamine and 1350 parts of N,N-dimethylformamide was stirred for 20 hours at 70° C. The reaction mixture was evaporated in vacuo and the residue was stirred in dichloromethane. The precipitate was filtered off. The filtrate was washed three times with 200 parts of water and once with 200 parts of a diluted ammonium hydroxide solution, dried, filtered and evaporated. The residue was purified by column chromatography over silical gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 58.9 parts (61.9%) of 1-[5,5-bis(4-fluorophenyl)-4-pentenyl]-4-(phenylmethyl)-2-piperazinecarboxamide as a residue (int. 33).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026853
Source datasetuspto-grants-1991_06
ORD IDord-c8cfe97ba2ee4f9eb5e94067af3f8e7a
Source noteuspto-grants-1991_06